PedAM
Pediatric Disease Annotations & Medicines
| Disease | epilepsy |
| Phenotype | C0002395|alzheimer disease |
| Sentences | 1 |
| PubMedID- 21822699 | Atypical presentation of a novel presenilin 1 r377w mutation: sporadic, late-onset alzheimer disease with epilepsy and frontotemporal atrophy. |
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